Computer System Validation

Validation & Engineering Group

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Manati, PR, pr on site Until 8/22/2026 First posted March 27, 2025 Last posted March 27, 2025
Job description

Validation & Engineering Group, Inc is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services in Puerto Rico and USA.

• URS development, routing for approval and DCA process • DCA Management (Request doc numbers, upload, approval and route for approval) • Systems
Impact Assessment. Be advice that Engineering impact assessment and CSV impact
assessment are two different forms. • Maximo CMMS o Data Entry into Maximo CMMS o Spare Parts(must include all necessary parts such as but not limited
to: instruments temperature/humidity, calibration form, chart recorder, fuses, relays, breakers, boards etc) o Job Plan/PM (Electrical & Mechanical) o Equipment
& Instrument Forms o Job Plan Trainings • Commissioning protocol development, routing for approval, execution and DCA process • Include a characterization
test as part of the commissioning • Commissioning protocol report development, routing for approval and DCA process • Risk assessment development,
routing for approval and DCA process • Validation Plan development/routing for approval and DCA process • IOQ protocol development, execution routing for
review/approval. Including associated completion forms per each stage(IQ, OQ) as per V-S-001 • Contractor must install data loggers for temperature and
humidity mapping • Contractor must download recorded data from data loggers to confirm that the test is in compliance with protocol requirements • Up to 3
document revisions must be included( 3 offline revision, 3 approval process revision) • Initial and final Traceability matrix development, execution, approval and
DCA process. • TM Report • VP Report • IOQ Report • Data mapping & Data flow protocol development routing for approval and associated report as
applicable including DCA management • Removal of existing control panel spare parts from CMMS system. • TOP: Turn Over Package development,
execution and completion. • SOP’S: one administrative SOP and one Operational SOP • CSV/IT job plan review to include yearly backup generation • Change
control management: development, presentation for endorsement, change action documentation and change control closing • QBAS & BAS scope: this
chamber has temperature and humidity signals that are reported to QBAS/BAS system as part of the scope contractor must: o Format and upload to DCA:
SAT, DS associated to BAS o Execute SAT with Honeywell o Develop SAT report including associated form o DCA management for SAT protocol & report

Positions available for Puerto Rico.

Validation and Engineering Group, Inc is an Equal Employment Opportunity employer.

About this role

Summary

Perform validation, commissioning, risk assessment, and documentation for pharmaceutical systems.

Job title

Computer System Validation

Experience level

Industry

pharmaceutical

Location requirements

Manati, PR; on-site role with some remote tasks allowed.

Salary

Not specified

Management role

No

Skills & keywords

Required skills

URS developmentDCA managementMaximo CMMScommissioningvalidation planIOQ protocolrisk assessment

Preferred skills

None specified

Specializations

URS developmentDCA managementMaximo CMMScommissioningrisk assessment
Locations

Structured locations inferred from the posting.

Manatí, 00674, Puerto Rico

On-site City